PINK1 and Parkin mitochondrial quality control: a source of regional vulnerability in Parkinson's disease

P Ge, VL Dawson, TM Dawson - Molecular neurodegeneration, 2020 - Springer
That certain cell types in the central nervous system are more likely to undergo
neurodegeneration in Parkinson's disease is a widely appreciated but poorly understood …

Autophagy in Parkinson's disease

X Hou, JO Watzlawik, FC Fiesel, W Springer - Journal of molecular biology, 2020 - Elsevier
Impaired protein homeostasis and accumulation of damaged or abnormally modified protein
are common disease mechanisms in many neurodegenerative disorders, including …

Environmental pollutants as risk factors for neurodegenerative disorders: Alzheimer and Parkinson diseases

M Chin-Chan, J Navarro-Yepes… - Frontiers in cellular …, 2015 - frontiersin.org
Neurodegenerative diseases including Alzheimer (AD) and Parkinson (PD) have attracted
attention in last decades due to their high incidence worldwide. The etiology of these …

Mitochondrial dysfunction in Parkinson's disease: molecular mechanisms and pathophysiological consequences

N Exner, AK Lutz, C Haass, KF Winklhofer - The EMBO journal, 2012 - embopress.org
Neurons are critically dependent on mitochondrial integrity based on specific morphological,
biochemical, and physiological features. They are characterized by high rates of metabolic …

[HTML][HTML] Mitochondrial dysfunction in Parkinson's disease

KF Winklhofer, C Haass - Biochimica et Biophysica Acta (BBA)-Molecular …, 2010 - Elsevier
Mitochondria are highly dynamic organelles which fulfill a plethora of functions. In addition to
their prominent role in energy metabolism, mitochondria are intimately involved in various …

Parkinson's disease

B Thomas, MF Beal - Human molecular genetics, 2007 - academic.oup.com
Parkinson's disease (PD) is a chronic progressive neurodegenerative movement disorder
characterized by a profound and selective loss of nigrostriatal dopaminergic neurons …

Expanding insights of mitochondrial dysfunction in Parkinson's disease

PM Abou-Sleiman, MMK Muqit, NW Wood - Nature Reviews …, 2006 - nature.com
The quest to disentangle the aetiopathogenesis of Parkinson's disease has been heavily
influenced by the genes associated with the disease. The α-synuclein-centric theory of …

The role of parkin in familial and sporadic Parkinson's disease

TM Dawson, VL Dawson - Movement disorders, 2010 - Wiley Online Library
Mutations in parkin are the second most common known cause of Parkinson's disease (PD).
Parkin is an ubiquitin E3 ligase that monoubiquitinates and polyubiquitinates proteins to …

Parkin loss leads to PARIS-dependent declines in mitochondrial mass and respiration

DA Stevens, Y Lee, HC Kang, BD Lee… - Proceedings of the …, 2015 - National Acad Sciences
Mutations in parkin lead to early-onset autosomal recessive Parkinson's disease (PD) and
inactivation of parkin is thought to contribute to sporadic PD. Adult knockout of parkin in the …

Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseases

JMM Tan, ESP Wong, DS Kirkpatrick… - Human molecular …, 2008 - academic.oup.com
Although ubiquitin-enriched protein inclusions represent an almost invariant feature of
neurodegenerative diseases, the mechanism underlying their biogenesis remains unclear …